Minoxidil
- Product NDC
- 59726-115
- 11-digit product format
- 597260115
- Labeler code
- 59726
- Product ID
- 59726-115_718a6b1f-b594-488d-8b9d-00891cb478f3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- P & L Development, LLC
- Application
- ANDA208092
- Marketing category
- ANDA
- Marketing start
- 2023-05-05
- Substance
- MINOXIDIL
- Active strength
- 50 mg/g
- Pharmacologic classes
- Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 5965120SH1 | MINOXIDIL | 38304-91-5 | MINOXIDIL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 59726-115-60 | 59726011560 | 60 g in 1 CAN (59726-115-60) | 60 g | 2023-05-05 | No | No | Historical |
| 59726-115-65 | 59726011565 | 2 CAN in 1 PACKAGE (59726-115-65) / 60 g in 1 CAN | 2 can | 2023-05-05 | No | No | Historical |
| 59726-115-70 | 59726011570 | 3 CAN in 1 PACKAGE (59726-115-70) / 60 g in 1 CAN | 3 can | 2023-05-05 | No | No | Historical |